A Tribute for World Down Syndrome Day: March 21, 2023

For those who don’t know, today is World Down Syndrome Day.  I new friend wrote this wonderful tribute that I want to share with each of you.  I hope you will share it with your friends.

Thanks for caring.

Grace’s Dad

Scott Schara, President

Our Amazing Grace ™

1 Sam 17:47

Our Amazing Grace is a trademark of Our Amazing Grace’s Light Shines On, Inc.

Grace Schara

WORLD DOWN SYNDROME DAY
&
AMAZING GRACE
 
By Julie Grimstad
March 21, 2023
 
A joyful heart is the health of the body,
but a depressed spirit dries up the bones.
~ Proverbs 17:22
 

Today is World Down Syndrome Day.

Few babies with Down syndrome and other chromosome disorders survive the womb. Most of them are victims of abortion, an evil permitted by a culture that measures the value of life in terms of “perfection” and “the ability to contribute to society”. Nevertheless, the families of children with Down syndrome and other chromosome disorders almost universally state that their children bring them immense joy. Surely bringing joy, in a world gripped by so much depression, anxiety, and anger, is one of the greatest contributions to society that anyone can make!

Meet Amazing Grace

Recently, I received a call from Scott Schara, the father of Grace. Scott explained how his 19-year-old daughter who had Down syndrome was killed in a hospital that followed the government’s Covid treatment protocol. The tragic story of her death and the beautiful story of her life are both told on the website www.OurAmazingGrace.net. This website was created “to help wake us up to what’s happening in many hospitals today and turn us to the only One who can truly fix this mess.” That is an extremely important message. I urge you to visit Grace’s website and learn more. However, today is a day to celebrate the lives of people with Down syndrome and Grace’s brief life is truly worth celebrating.

Grace was the heart of her family. Her mother, Cindy, wrote in her obituary,

“She had a way of brightening up a room just by her presence. Many have told us they will miss her bright, contagious smile, her happy laugh, her silly antics as she was always trying to sneak up behind someone, her sharp mind and her generous nature. Those things and so much more will be hard to live without. Having Grace here with us was like having a bit of heaven on earth.”

Standing with the Down Syndrome Community

Today, HALO stands with the worldwide Down syndrome community, seeking full inclusion for people with Down syndrome in all areas of life. In particular, because of HALO’s special concern for the medically vulnerable, we advocate for better access to good medical care, as well as protection for the lives of people with Down Syndrome, born and preborn.
 

Want to Help HALO and be 
a Voice for the Medically Vulnerable?

DONATE NOW

Thank you for your support! Our organization is a 501 (c)(3) organization. Donations are tax-deductible to the extent allowed by law.
 

If you would like to donate through the mail, please send checks only to:
HALO, 7301 Bass Lake RD, Minneapolis, MN 55428.

MISSION STATEMENT

The Healthcare Advocacy and Leadership Organization (HALO) is a voice for the medically vulnerable. As a non-profit, Christian organization, HALO addresses a wide array of ethical issues including euthanasia, assisted suicide, rationing of medical services, and hastening of death in healthcare settings. In addition, HALO promotes life-affirming healthcare practices, life-protective advance directives, and compassionate care for the sick and those nearing the end of their lives. In all circumstances, HALO espouses in healthcare practice the sanctity and integrity of every human person.

HALO accomplishes its mission through intercessory prayer; widespread education; community awareness and assistance programs; interaction with patients, families, and caregivers; and referrals to appropriate resources when necessary.